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Establishing patient-derived organoids from human endometrial cancer and normal endometrium
Endometrial cancer is the most common gynecologic malignancy in the United States and is one of the few malignancies that had an increasing incidence and mortality rate over the last 10 years. Current research models fail to recapitulate actual characteristics of the tumor that are necessary for the...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10140435/ https://www.ncbi.nlm.nih.gov/pubmed/37124727 http://dx.doi.org/10.3389/fendo.2023.1059228 |
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author | Katcher, Arielle Yueh, Brian Ozler, Kadir Nizam, Aaron Kredentser, Ariel Chung, Charlie Frimer, Marina Goldberg, Gary L. Beyaz, Semir |
author_facet | Katcher, Arielle Yueh, Brian Ozler, Kadir Nizam, Aaron Kredentser, Ariel Chung, Charlie Frimer, Marina Goldberg, Gary L. Beyaz, Semir |
author_sort | Katcher, Arielle |
collection | PubMed |
description | Endometrial cancer is the most common gynecologic malignancy in the United States and is one of the few malignancies that had an increasing incidence and mortality rate over the last 10 years. Current research models fail to recapitulate actual characteristics of the tumor that are necessary for the proper understanding and treatment of this heterogenous disease. Patient-derived organoids provide a durable and versatile culture system that can capture patient-specific characteristics such as the mutational profile and response to therapy of the primary tumor. Here we describe the methods for establishing, expansion and banking of endometrial cancer organoids to develop a living biobank. Samples of both endometrial tumor tissue and matched normal endometrium were collected from 10 patients. The tissue was digested into single cells and then cultured in optimized media to establish matched patient endometrial cancer and normal endometrial tissue organoids. Organoids were created from all major endometrial cancer histologic subtypes. These organoids are passaged long term, banked and can be utilized for downstream histological and genomic characterization as well as functional assays such as assessing the response to therapeutic drugs. |
format | Online Article Text |
id | pubmed-10140435 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101404352023-04-29 Establishing patient-derived organoids from human endometrial cancer and normal endometrium Katcher, Arielle Yueh, Brian Ozler, Kadir Nizam, Aaron Kredentser, Ariel Chung, Charlie Frimer, Marina Goldberg, Gary L. Beyaz, Semir Front Endocrinol (Lausanne) Endocrinology Endometrial cancer is the most common gynecologic malignancy in the United States and is one of the few malignancies that had an increasing incidence and mortality rate over the last 10 years. Current research models fail to recapitulate actual characteristics of the tumor that are necessary for the proper understanding and treatment of this heterogenous disease. Patient-derived organoids provide a durable and versatile culture system that can capture patient-specific characteristics such as the mutational profile and response to therapy of the primary tumor. Here we describe the methods for establishing, expansion and banking of endometrial cancer organoids to develop a living biobank. Samples of both endometrial tumor tissue and matched normal endometrium were collected from 10 patients. The tissue was digested into single cells and then cultured in optimized media to establish matched patient endometrial cancer and normal endometrial tissue organoids. Organoids were created from all major endometrial cancer histologic subtypes. These organoids are passaged long term, banked and can be utilized for downstream histological and genomic characterization as well as functional assays such as assessing the response to therapeutic drugs. Frontiers Media S.A. 2023-04-14 /pmc/articles/PMC10140435/ /pubmed/37124727 http://dx.doi.org/10.3389/fendo.2023.1059228 Text en Copyright © 2023 Katcher, Yueh, Ozler, Nizam, Kredentser, Chung, Frimer, Goldberg and Beyaz https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Endocrinology Katcher, Arielle Yueh, Brian Ozler, Kadir Nizam, Aaron Kredentser, Ariel Chung, Charlie Frimer, Marina Goldberg, Gary L. Beyaz, Semir Establishing patient-derived organoids from human endometrial cancer and normal endometrium |
title | Establishing patient-derived organoids from human endometrial cancer and normal endometrium |
title_full | Establishing patient-derived organoids from human endometrial cancer and normal endometrium |
title_fullStr | Establishing patient-derived organoids from human endometrial cancer and normal endometrium |
title_full_unstemmed | Establishing patient-derived organoids from human endometrial cancer and normal endometrium |
title_short | Establishing patient-derived organoids from human endometrial cancer and normal endometrium |
title_sort | establishing patient-derived organoids from human endometrial cancer and normal endometrium |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10140435/ https://www.ncbi.nlm.nih.gov/pubmed/37124727 http://dx.doi.org/10.3389/fendo.2023.1059228 |
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